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N,N-Diethylaniline → HCID 54342542, 화합물

HRID 1858316
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HRID 1858316 반응식
Cl[C:2]1[C:7]([CH2:8][NH:9][C:10]2[C:15]([Cl:16])=[CH:14][CH:13]=[CH:12][C:11]=2[Cl:17])=[CH:6][N:5]=[C:4]([S:18][CH3:19])[N:3]=1.[C:20]([O:24][C:25](=[O:38])[NH:26][C:27]([CH3:37])([CH3:36])[CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([NH2:35])[CH:30]=1)([CH3:23])([CH3:22])[CH3:21].C(N(CC)C1C=CC=CC=1)C>ClCCl>[C:20]([O:24][C:25](=[O:38])[NH:26][C:27]([CH3:37])([CH3:36])[CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([NH:35][C:2]2[C:7]([CH2:8][NH:9][C:10]3[C:15]([Cl:16])=[CH:14][CH:13]=[CH:12][C:11]=3[Cl:17])=[CH:6][N:5]=[C:4]([S:18][CH3:19])[N:3]=2)[CH:30]=1)([CH3:23])([CH3:21])[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7061N,N-DiethylanilineHCID 221250524-Chloro-5-(2,6-dichloroanilinomethyl)-2-methylthiopyrimidineHCID 226740811,1-Dimethylethyl N-[2-(3-aminophenyl)-1,1-dimethylethyl]carbamate

생성물 1

HCID 54342542HCID 54342542, 화합물수율 39%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 520 mg (1.6 mmol) of 4-chloro-5-(2,6-dichloroanilinomethyl)-2-methylthiopyrimidine, 420 mg (1.6 mmol) of (2-(3-aminophenyl)-1,1-dimethyl-ethyl)-carbamic acid tert-butyl ester and 250 mg (1.7 mmol) of N,N-diethylaniline in 5 ml of dichloromethane was heated at 80° C. until the solvent had evaporated and then to 120° C. for 30 minutes and then cooled. The product was purified by flash chromatography on silica gel eluting with diethyl ether/isohexane in a ratio 1:1 to give 350 mg (39%) of (2-(3-[5-[(2,6-dichlorophenylamino)-methyl]-2-methylthiopyrimidin-4-yl-amino]-phenyl)-1,1-dimethyl-ethyl)-carbamic acid tert-butyl ester as a white solid. [Mass spectrum (ESI) MH+ =562].

후처리

  1. customhad evaporated
  2. temperaturecooled
  3. customThe product was purified by flash chromatography on silica gel eluting with diethyl ether/isohexane in a ratio 1:1

출처 및 근거

ORD 기록
ord-896be482f22f46c2ad5d38bf43600a09
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06150373

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